de Gaudemaris, G. published the artcilep-Iodobenzohydrazide: a reagent for the carbonyl group, Recommanded Product: 4-Iodobenzohydrazide, the publication is Bulletin de la Societe Chimique de France (1950), 63-5, database is CAplus.
p-IC6H4CONHNH2, prepared by the method of Sah and Hsü (C.A. 35, 4362.8), reacts with carbonyl groups in EtOH at 95° in the presence of a small amount of HOAc to give p-iodobenzoylhydrazones. These products are analyzed for iodine by reaction with Na (Drogin and Rosanoff, C.A. 10, 871) and a subsequent Volhard titration Derivatives were prepared of pinacolone, m. 154°; ethylpinacolone, m. 146-7°; iso-BuCOMe, m. 136°; Me nonyl ketone, m. 118°; MeCH:CHCOMe, m. 183-4°; MeCH:CMeCOMe, m. 158-60°; mesityl oxide, m. 141-2°; MeCHCMe:CMeCOMe, m. 138°; Me2C(OH)COMe, m. 84-5°; Et2C(OH)COMe, m. 135-6°; benzoin, m. 194°; EtCH(OH)COMe, m. 133-4°; MeCH(OH)CHMeCOMe, m. 150°; and the tertiary β-ketols prepared by Dubois (C.A. 43, 5004d) from Me2CO, MeCOC6H13, Pr2CHCOMe, and pinacolone, m. 110-12°, 167-8°, 142° and 164°, resp.
Bulletin de la Societe Chimique de France published new progress about 39115-95-2. 39115-95-2 belongs to iodides-buliding-blocks, auxiliary class Iodide,Hydrazine,Amine,Benzene,Hydrazide,Amide, name is 4-Iodobenzohydrazide, and the molecular formula is C7H7IN2O, Recommanded Product: 4-Iodobenzohydrazide.
Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com